Clearance Summary
GILLETTE HEAT WRAP received FDA 510(k) clearance under submission number K790374, sponsored by The Gillette Company. The device was reviewed via the Traditional premarket notification pathway and assigned to the Physical Medicine review panel. The statutory decision date of record is 1979-04-10.
- Submission: K790374
- Applicant / Sponsor: The Gillette Company
- Clearance pathway: Traditional
- Review panel: Physical Medicine
- Device class: Class II
- Regulation citation: 21 CFR 890.5740
- Decision date: 1979-04-10
Classification & Regulation
This clearance is catalogued under FDA product code IRT and 21 CFR 890.5740, within the Physical Medicine review panel as a Class II device.